Demonstrates expertise in medical data review and eligibility review, with a strong understanding of oncology and GYN therapeutic areas. Capable of managing project scope, timelines, and deliverable quality while ensuring adherence to clinical practices and data privacy guidelines.

Highest-signal resume keywords

Medical Data Review ExperienceOncology KnowledgeProject Management SkillsGood Clinical Practices (GCP)Data Privacy Guidelines Adherence

About the role

Key responsibilities & impact

Work with the Medical Director to develop medical plans, including Medical Management, Medical Data Review, and Eligibility Review Plans
Engage outside experts, consultants, and advisors to coordinate necessary medical/scientific input
Perform regular and ad-hoc medical review of data listings and data visualizations
Analyze data to identify risks and data patterns/trends and document medical reviews
Identify and resolve medical data review issues
Author medical data queries, review responses, and approve query closure with the Medical Director
Assist with patient profile reviews, scientific review of study-level data, protocol deviation review, and Medical Review Summary reports
Partner with Medical Directors on medical data review and safety review meetings, including slide preparation
Manage project scope, objectives, deliverable quality, milestones, and timelines
Serve as primary interface between internal teams, customers, and vendors for medical data and eligibility review
Collaborate with study teams to identify data integrity and subject safety risks
Escalate study concerns, at-risk deliverables, and out-of-scope tasks to project leads
Attend and present at Trusted Process meetings and participate in audits
May manage a limited number of direct reports and participate in or conduct interviews

Requirements

What you’ll need

Equivalent experience, skills, and/or education will also be considered
Basic understanding and knowledge of ongoing protocol designs and disease related terminology and pathology
Adherence to data privacy guidelines, International Committee on Harmonization (ICH), Good Clinical Practices (GCPs), enterprise policies, standard operating procedures, work instructions, and project plans
Ability to collaborate with Clinical Operations, Data Management, Drug Safety and Pharmacovigilance, and Project Management
Ability to manage project scope, objectives, quality of deliverables, milestones, and timelines
Ability to attend and present at Trusted Process meetings and participate in internal and external audits
Medical data review and eligibility review experience implied by the listed responsibilities
Oncology and GYN therapeutic-area knowledge implied by the role title and responsibilities

Benefits

Comp & perks

career development and progression
supportive and engaged line management
technical and therapeutic area training
peer recognition and total rewards program
Inclusive culture
Company car or car allowance
Medical, Dental and Vision health benefits
Company match 401k
Eligibility to participate in Employee Stock Purchase Plan
Eligibility to earn commissions/bonus based on company and individual performance
Flexible paid time off (PTO) and sick time

ATS Keywords

✓ Tailor your resume

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills

Medical ManagementData AnalysisMedical Data QueriesData VisualizationProtocol Deviation ReviewMedical Review Summary ReportsRisk IdentificationEligibility Review PlansScientific ReviewData Integrity Assessment

Soft Skills

CollaborationCommunicationProblem-SolvingLeadershipPresentation Skills

Industry Keywords

International Committee on Harmonization (ICH)Clinical OperationsDrug SafetyPharmacovigilanceTrusted Process Meetings